CALR3
Calreticulin-3
Also known as: CALR3_HUMAN, CRT2, CT93, FLJ25355, MGC26577
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96L12
- Gene
- CALR3
- Ensembl
- ENSG00000269058
- Chromosome
- 19
- Canonical length
- 384 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
The protein encoded by this gene belongs to the calreticulin family, members of which are calcium-binding chaperones localized mainly in the endoplasmic reticulum. This protein is also localized to the endoplasmic reticulum lumen, however, its capacity for calcium-binding may be absent or much lower than other family members. This gene is specifically expressed in the testis, and may be required for sperm fertility. Mutation in this gene has been associated with familial hypertrophic cardiomyopathy. [provided by RefSeq, Dec 2011]
Canonical amino-acid sequenceUniProt
384 residues, UniProt reviewed canonical sequence.
>Q96L12|CALR3
1 MARALVQLWA ICMLRVALAT VYFQEEFLDG EHWRNRWLQS TNDSRFGHFR LSSGKFYGHK
61 EKDKGLQTTQ NGRFYAISAR FKPFSNKGKT LVIQYTVKHE QKMDCGGGYI KVFPADIDQK
121 NLNGKSQYYI MFGPDICGFD IKKVHVILHF KNKYHENKKL IRCKVDGFTH LYTLILRPDL
181 SYDVKIDGQS IESGSIEYDW NLTSLKKETS PAESKDWEQT KDNKAQDWEK HFLDASTSKQ
241 SDWNGDLDGD WPAPMLQKPP YQDGLKPEGI HKDVWLHRKM KNTDYLTQYD LSEFENIGAI
301 GLELWQVRSG TIFDNFLITD DEEYADNFGK ATWGETKGPE REMDAIQAKE EMKKAREEEE
361 EELLSGKINR HEHYFNQFHR RNELLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CALR3 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.38
- Highest tissue expression
- 62 nTPM
Expression across tissuesHPA
Tissue
- testis: 62 nTPM
- epididymis: 0.8 nTPM
- fallopian tube: 0.1 nTPM
- thymus: 0.1 nTPM
- thyroid gland: 0.1 nTPM
- adipose tissue: 0 nTPM
Single-cell type
- early spermatids: 48 nCPM
- late primary spermatocytes: 16 nCPM
- late spermatids: 12 nCPM
- early primary spermatocytes: 2.3 nCPM
- differentiating spermatogonia: 0.6 nCPM
- epididymal efferent duct ciliated cells: 0.4 nCPM
Immune cell
- neutrophil: 0.4 nTPM
- memory B-cell: 0.2 nTPM
- naive B-cell: 0.2 nTPM
- naive CD4 T-cell: 0.1 nTPM
- plasmacytoid DC: 0.1 nTPM
- basophil: 0 nTPM
Brain region
- midbrain: 0.5 nTPM
- cerebral cortex: 0.4 nTPM
- hippocampal formation: 0.4 nTPM
- hypothalamus: 0.4 nTPM
- pons: 0.4 nTPM
- amygdala: 0.3 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.14
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.35
- DepMap mean gene effect
- -0.13
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CALR3 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CALR3 as an antibody target. Whether an autoantibody or antibody against CALR3 could matter depends on whether native CALR3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CALR3 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label CALR3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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